US 7935102 B2
A system for preventing air from entering a first catheter of a multi-catheter system. Air is prevented from entering the proximal end of the first catheter by an axially elongate chamber having an impeller, the chamber being affixed to the proximal end of the first catheter. The air is removed through a port near the centerline of the chamber. Liquid removed with the air is returned to the chamber to minimize liquid loss during the procedure. A second catheter inserted through the chamber and into the first catheter is unable to entrain gas into the first catheter because any gas that enters the chamber is routed to the centerline of the chamber where it is removed. Inflow of fluid from an external pump scrubs the second catheter shaft of air bubbles attached by surface tension.
1. A method for preventing gas from entering a catheter, wherein the catheter interior is exposed to blood or other liquid, said method comprising:
affixing an axially elongate shell at or near the proximal end of a first catheter, wherein said shell comprises a chamber having a centerline;
rotating an impeller about or near the centerline of the chamber, wherein said rotation of said impeller directly imparts rotational energy to a fluid within the chamber causing any gas collected within the chamber to migrate toward the centerline;
removing the gas from the chamber through a gas removal port near the centerline of said shell;
affixing a catheter inlet port to the shell near a periphery of said chamber, said catheter inlet port operably connected to the chamber;
affixing a catheter outlet port near the distal end of the shell, said catheter outlet port being affixed, and operably connected to the proximal end of the first catheter, and near a periphery of said chamber, wherein the catheter inlet port is coaxially aligned with the catheter outlet port;
inserting a second catheter through the catheter inlet port, through the chamber, through the catheter outlet port, through the first catheter, and on into the cardiovascular system of a patient; and
separating any liquid removed from the chamber from the gas.
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This application claims priority benefit under 35 USC §119(e) from U.S. Provisional Application No. 61/008,952, filed Dec. 21, 2007, entitled METHOD AND APPARATUS FOR PREVENTION OF CATHETER AIR INTAKE, and U.S. Provisional Application No. 61/069,979, filed Mar. 19, 2008, entitled METHOD AND APPARATUS FOR PREVENTION OF CATHETER AIR INTAKE the entire contents of both of which are hereby incorporated herein by reference.
The field of this invention is cardiology, radiology, electrophysiology, or endovascular surgery, and more particularly the fields of cardiac or circulatory system catheterization.
Catheters are introduced into the cardiovascular system for various diagnostic and therapeutic reasons. Catheters are often introduced into the cardiovascular system through introduction sheaths that provide a pre-determined conduit from the access site to the treatment site and facilitate vascular access of new catheters as well as the exchange of catheters within the vasculature. Such catheters and introducer sheaths are used in both the arterial, higher pressure, circulation and the venous, lower pressure, circulation. Introducer sheaths suitable for guiding devices through the vasculature and into the right or left atrium of the heart are prime examples of such vascular access.
The introducer sheaths and catheters used for these purposes are generally primed with saline and purged of any air prior to being inserted into the patient's cardiovascular system through a percutaneous or open surgical access to an artery or vein. The purpose of purging air from a catheter or introducer sheath is to prevent that air from inadvertently being forced, under a pressure drop generated within the catheter or sheath, out the distal end of the catheter and into the patient's circulatory system.
The act of inserting a therapeutic or diagnostic catheter through an introducer sheath can cause air or other gas to be introduced into the central lumen of the introducer sheath. Such air can migrate distally into the patient's cardiovascular system under certain circumstances, especially when the distal end of the introducer sheath is located within the venous side of the cardiovascular system or in the left atrium of the heart. In certain pathological and physiological states, relatively low pressures can exist within the venous side of the heart with a pressure gradient existing between the right and left atrium. Such gradients in the presence of a Patent Foramen Ovale (PFO), a not uncommon congenital cardiac condition, can easily result in air emboli traversing from the right heart to the left heart during right heart interventional procedures. In addition, these relatively low pressures can exist for a non-trivial portion of the cardiac cycle resulting in the potential for a negative pressure gradient between the room pressure, which in a clean room, catheterization lab, or surgical suite is generally slightly elevated, and the distal end of the introduction sheath. There is a potential for any gas or air entrained into the proximal end of the introduction sheath to migrate out the distal end of the introduction sheath and into the patient's cardiovascular system where it could cause an air embolism. During a portion of the cardiac cycle, pressures within the left atrium can approach very low values and can even go negative relative to room pressure.
The clinical ramifications of an air embolism range from no noticeable effect to cerebrovascular stroke or cardiac ischemia, either of which could have mild to severe outcomes and could even result in patient death. Air can also be entrained out the distal end of the sheath by surface tension forces between the catheter and the air. This surface tension can cause the air to adhere to the catheter while it is advanced out the distal end of the sheath. Thus, any air that inadvertently enters the sheath or catheter system is at risk for introduction to the patient, an event with potentially catastrophic consequences such as cerebrovascular embolism, coronary embolism, and the like. Air embolism is clearly an issue especially with catheters directed toward the cerebrovasculature or the coronary circulation, but also with catheters or sheaths directed anywhere within the circulatory system of the mammalian patient.
New devices and methods are needed to more efficiently remove gas that inadvertently migrates into a catheter or sheath so that it is prevented from being routed into the patient's cardiovascular system. The need has been heightened by recent Medicare regulations that restrict or deny reimbursement for certain hospital acquired conditions including air embolism.
This invention relates to a blood filter, blood-air filter, or trap for removing air or other gas from the fluid within a primed introducer sheath, catheter, or similar device placed anywhere within the cardiovascular circuit of a patient. The liquid fluid within a cardiovascular catheter or sheath can comprise blood, blood products, water, sodium chloride, various pharmacologic agents, and the like. In some embodiments of the inventions, the device or apparatus comprises a chamber or housing with a catheter inlet port and a catheter outlet port, the catheter outlet port being connected to the proximal end of an introduction sheath, or first catheter. In addition, the chamber has a third outlet port for removing gas from the liquid. The device additionally comprises a stirring rod or impeller to spin the blood circumferentially within the chamber. This stirring rod or impeller is coupled to a rotary motor that generates the rotational energy necessary to separate gas from the blood by buoyancy, or centripetal effects. The less dense bubbles move toward the center of the rotating fluid field while the more dense liquid is moved to the periphery of the rotating fluid field. The faster the fluid field rotates, the more quickly the air is separated from the liquid. The present inventions actively remove gas and debris from the catheter, including both tiny gas bubbles and large boluses of gas. The inventions can strip gas or air bubbles, attracted to a secondary catheter inserted through the chamber by surface tension effects or similar forces, away from the secondary catheter and into a rotational flow field where the gas can be actively removed from the chamber. The gas has less mass than the same volume of blood or saline, i.e. the bubbles are buoyant in the liquid, so that rotation causes them to move toward the center of the liquid filter by centripetal force. The centripetal force accelerates the gas until the bubbles reach an axially inward radial velocity where the drag force balances the centrifugal force and the bubbles move toward the center of rotation of the device.
In some embodiments, the invention actively rotates the blood or other liquid within a chamber to drive gas toward the center of the chamber under centrifugal forces interacting with buoyant forces on the gas, and allows separation of the blood or other liquid from the aforementioned gas. The gas is removed from the chamber of the device through a gas vent, approximately aligned with the axis of rotation, where the air is stored in a gas reservoir, while any liquid is pumped back into the chamber of the device. The gas trap or filter of the present invention is designed to remove the majority of air bubbles and prevent those air bubbles from entering or escaping the distal end of the catheter or sheath.
In some embodiments, the axis of the chamber, and the axis about which the impeller rotates, is aligned parallel to the longitudinal axis of the catheter or sheath to which it is affixed. In another embodiment, the chamber is aligned with its rotational axis lateral to that of the catheter major axis. In this embodiment, rotational fluid flow is less restricted by the presence of a catheter being inserted along the longitudinal axis of the sheath because the inserted catheter, which passes through the chamber is aligned generally in the direction of the rotational fluid flow and not transverse thereto.
In another embodiments, the chamber does not comprise an impeller but the chamber comprises an inlet seal or valve that separates the chamber from the outside environment, an optional outlet seal or valve that separates the chamber from the distal end of the first catheter or sheath, an outlet port for air and a return port for liquids. The inlet seal or valve and the outlet seal or valve serve to trap any air within the chamber so that the air cannot pass into the proximal end of the sheath or catheter through the outlet valve or seal. The chamber further comprises an external fluid pump, air reservoir, return line, and electrical power source.
In some embodiments, a filter is described that is affixed or integral to the proximal end of an introducer or introduction sheath. The filter is completely self-contained, small, and non-bulky. The filter, including all components, can be contained or integrated within a shell. The filter, including all components, can be contained either within a shell or within modules directly affixed to the shell. In certain embodiments, the filter is a unitary or integral structure with no wires, lines, tubes, or other flexible linkages extending therefrom. The filter system does not require a hanging bag or reservoir of saline or other liquid since it gets its fluid from the catheter itself. The filter is capable of being maneuvered at the proximal end of the sheath and allows therapeutic or diagnostic catheters to be passed therethrough on their way into the sheath or introducer. Thus, all components or modules are integral to, or affixed to, the filter unit. The components or modules can all be integrated within or housed within a single shell, casing. This is extremely important so that the filter assembly does not render the sheath or catheter system unwieldy, awkward, or unbalanced. In certain embodiments, the chamber, the return line, the air separation chamber, the pump, the pump motor, the battery, any inlet and outlet valves, and all interconnecting components are integral to or affixed to each other. The components can be rigidly or flexibly affixed to each other. The battery can comprise chemistries such as, but not limited to, alkaline, lithium, lithium ion, nickel metal hydride, lead acid, and the like. Battery operating voltages can range between 1.25 and 12 volts with a preferred range of between 3 and 7 volts. Computers, controllers, and other circuitry can be used to monitor motor function, presence of gas via ultrasound transducers, battery power, and the like. The controllers can further comprise circuitry, software, or both to process the information and provide warnings to the user.
In accordance with another aspect of the invention, a method is described to remove gas from an axially elongate chamber affixed to the proximal end of an introducer, first catheter, or introduction sheath. This method includes the step of affixing the chamber to the proximal end of the first catheter or sheath such that the first catheter or sheath is connected near the radial periphery of the chamber. Next the method includes spinning the fluid, blood, saline, air, and the like, within the chamber about a central axis by means of an impeller at high rotational rates to move the gas to the center, or axis of rotation, of the chamber and away from the first catheter or sheath port to a gas removal port located generally near the axis of rotation within the chamber where the gas is removed. In a further aspect of the invention, the air or gas removed from the fluid at or near the center of the chamber is separated from the liquid in an external gas separation chamber and the liquid is ultimately returned to the chamber or the patient. In an embodiment, the same impeller that spins the blood within the chamber can be used to pump the liquid back into the chamber. In another embodiment, a separate impeller or pump can be used to move the liquid back into the chamber. In another embodiment, the same motor but different impellers or pumping devices can be used to spin the blood and move the blood through the system.
In other embodiments, the chamber is configured so that fluid, blood, air, non-cellular prime, or the like, are pumped out of the chamber where the air is separated from the liquid, and the liquid is returned to the chamber. In yet another embodiment, entry and exit valves are provided at the proximal and distal end of the chamber. These entry and exit valves minimize the amount of fluid, either air or liquid that can escape therethrough, with or without a secondary catheter having been passed through these valves. In some embodiments, the return line to the chamber is aligned tangentially to the circumference of the chamber such that the return flow generates rotational flow within the chamber that strips air from a secondary catheter inserted therethrough and drives the air toward the center of the chamber where it is drawn off. In some of these embodiments, the chamber is aligned with its axis of rotation vertical so that the air or gas directed toward the center can rise and be removed out the exit vent from the chamber. In some embodiments, the top of the generally cylindrical chamber can have a domed, funnel, or otherwise tapered shape to coerce gas and air toward the center, where the fluid exit from the chamber is located.
The present inventions distinguish over the cited prior art because they use an active component, or tangential return flow jet, to spin the liquid to forcibly remove gas and gas bubbles from the blood, catheter prime, saline, or other liquid. The invention is most useful during endovascular surgery, interventional neuroradiology procedures, interventional cardiology procedures, electrophysiology procedures, and the like. The invention does not block air from entering a bubble filter chamber by application of high pressure but rather quickly removes air entrained into the chamber away from the catheter where it can be pulled off and separated from any liquid, thus allowing the air-free liquid to be returned to the system. The system also has the advantage, due to the high rotational velocity of the liquid within the chamber, of being able to scrub any air away from a second catheter inserted through the chamber, wherein the air is adherent to the catheter by surface tension effects.
In another embodiment of the invention, an ultrasound transducer is affixed to the chamber and the ultrasound transducer is connected to control circuitry such that the presence of air can be detected and a warning device such as an audible bell, buzzer, a visible light or warning device, or the like can be activated to alert the operator that air is within the system and that caution should be maintained or corrective steps applied. The ultrasound transducer can be made to monitor the chamber inlet, the chamber, outlet, or both such that, in an embodiment, the warning signal only occurs if air nears the outlet of the chamber, where it could potentially pass into the first catheter or sheath. Once the gas or air is detected, system checks can be performed to prevent any flushing of fluid and air, within a guide sheath and/or catheter, into the patient.
In other embodiments of the invention, the system is self-priming and withdraws liquid retrograde through the sheath and into the bubble filter such that it does not require a separate source of liquid or fluid. Such separate sources of liquid or fluid, which are not required for the present device or method, can include bags or reservoirs of fluid hung beside the patient. In some embodiments, the system comprises a valve at its proximal end but not at its distal end. In other embodiments, the system comprises a valve at both the proximal end and the distal end. The valve can be a hemostasis valve of the type including, but not limited to, a duckbill valve, a pinhole valve, a slit valve, a Tuohy-Borst valve, and the like. Any valves located at the distal end of the bubble filter are preferably able to permit retrograde flow therethrough, even with a secondary catheter inserted therethrough. Such retrograde flow capability facilitates priming of the filter with blood withdrawn from the patient. Any valves located at the proximal end of the bubble or air filter preferably seal both in the antegrade and retrograde directions.
In other embodiments, an external bubble collection system is provided outside the bubble or air filter. Air removed from the air or bubble filter main chamber, through which the secondary catheter passes, is moved through the external bubble collection system. The external bubble collection system can comprise a mesh filter having a pore size of about 25 microns and can further comprise a gravity separator to remove air from a high port while blood or non-cellular liquids are removed through a lower port. The external bubble collection system can further comprise a membrane filter operating under pressure to separate gas from liquid.
The present invention distinguishes over the cited prior art because it uses an active component to spin the blood to forcibly remove gas bubbles from the blood. The invention is useful during cardiovascular catheterization procedures, especially those accessing the left atrium, the venous circulation, and the cerebrovasculature. The device is also useful during surgery when cardiopulmonary bypass is instituted to maintain the patient on temporary cardiopulmonary support. It is also useful for removal of gas and bubbles during intravenous infusion of liquids to a patient. Patients with increased risk of pulmonary emboli are especially vulnerable during intravenous infusion and would benefit from such protection.
For purposes of summarizing the invention, certain aspects, advantages and novel features of the invention are described herein. It is to be understood that not necessarily all such advantages may be achieved in accordance with any particular embodiment of the invention. Thus, for example, those skilled in the art will recognize that the invention may be embodied or carried out in a manner that achieves one advantage or group of advantages as taught herein without necessarily achieving other advantages as may be taught or suggested herein.
A general architecture that implements the various features of the invention will now be described with reference to the drawings. The drawings and the associated descriptions are provided to illustrate embodiments of the invention and not to limit the scope of the invention. Throughout the drawings, reference numbers are re-used to indicate correspondence between referenced elements.
As used herein the terms distal and proximal are used to clarify the location of various points along the axial length of a catheter or sheath. Points are defined with respect to the end grasped by the user and the end that is inserted in the patient in the same manner as would one skilled in the art of medical device catheter construction. The proximal end of the catheter or sheath is defined as that end closest to the user or operator, or user, of the catheter or sheath while the distal end of the catheter or sheath is defined as that end that is inserted into the patient.
The shell 102 is configured with an axis of rotation about which fluid within the shell 102 can rotate. Therefore the shell 102 is approximately round in internal cross-section with the chamber 104 having a generally axially elongate cylindrical shape. The impeller 118 is affixed to the shaft of the motor drive (not shown) and rotates about the shaft axis at speeds between approximately 10 and 5000 revolutions per minute (RPM), and preferably between 100 and 1000 RPM. The primary concern is for removal of larger air bubbles that can be easily moved to the center of the device at these rotational rates, even if the device is flipped sideways, upside down, or any other orientation since the rotational, buoyant—forces will overpower gravitational at these rotation rates. The second catheter inlet port 110 is aligned generally tangential to the outer circumference of the chamber 104 and the lumen of the second catheter inlet port 110 is operably connected to the interior of the chamber 104. The second catheter outlet port 108 is aligned generally tangential to the outer circumference of the chamber 104 and is aligned generally coaxially with the second catheter inlet port 110. A second catheter 116, further comprising a second catheter hub 114 and a second catheter shaft 140, when inserted through the second catheter inlet port 110 can be advanced through the chamber 104 and into the second catheter outlet port 108 without restriction, binding, or obstruction. The entry 142 to the second catheter outlet port 108 from the chamber 104 can, in a preferred embodiment, be flared, beveled, or funnel shaped such that should the second catheter shaft 140 bend slightly out of the line of the straight axis, it will be coerced or guided into the second catheter outlet port 108.
The main axis, along which the second catheter 116 runs, can be oriented parallel to the rotational axis of the impeller 118 or, in a preferred embodiment, the catheter axis can be oriented perpendicular to the rotational axis of the impeller 118. The rotational axis of any fluid within the chamber 104 will be approximately the same as that of the impeller 118, since the impeller 118 directly drives the rotational motion of said fluid. By orienting the catheter 116 axis perpendicular to the rotational axis of the impeller 118, the blood and fluid within the chamber 104 will rotate generally in a similar direction as the axis of the second catheter shaft 140 as it passes the second catheter shaft 140 and thus flow disturbance by the catheter shaft 140 will be minimized. High velocity flow passing the second catheter shaft 140 will entrain any bubbles of gas attached thereto and drive the bubbles into the flow vortex created by the spinning impeller 118. The bubbles entrained in the flow vortex will migrate to the center of the vortex by buoyancy effects operating within the rotational flow field. Thus the lighter gas elements or bubbles will move inward while the heavier liquid and solid elements will move outward in the rotational flow field. The axis of rotation of the impeller 118 is preferably higher than the axis of the second catheter 116 so that passive buoyancy effects facilitate bubble separation from the region of the second catheter 116.
The shell 102 and the impeller 118 can be fabricated from polymers such as, but not limited to, polycarbonate, polysulfone, polyvinyl chloride, polyurethane, polyethylene, polyimide, polyamide, polyester, and the like. The shell 102 is preferably fabricated from a generally transparent polymer so that visualization of air or gas within the chamber 104 is possible. The diameter of the chamber 104 can range from about 0.5-cm to about 10-cm with a preferred diameter of about 2-cm to about 5-cm. The width of the chamber 104 along its rotational axis can range from about 1-cm to about 10-cm with a preferred range of about 2-cm to about 7-cm. The weight of the filter assembly 100 should be as low as possible so as to minimize forces on the first catheter or sheath 144 to which the filter assembly 100 is attached. The weight of the filter assembly 100 should be less than 450 grams and preferably less than 200 grams. The outlet port 108 of the filter assembly 100 can be attached to the first catheter or sheath 144 with a reversible coupling 146 such as a Luer lock, bayonet mount, screw thread, fastener, or the like, or it can be permanently affixed thereto. It is beneficial to use a locking type connector 146, or a permanent connection, to minimize the risk of the filter assembly 100 from inadvertently becoming disconnected from the first catheter or sheath 144 as air could then enter the first catheter or sheath 144, defeating the purpose of the filter assembly 100.
The valve 112 can be affixed, or integral, to the second catheter inlet port 110, which is affixed, or integral, to the chamber 104. The valve 112 can be a Tuohy-Borst valve, an elastomeric membrane with a pinhole, a duckbill valve, an elastomeric gasket with a central orifice slightly smaller than shaft 140 of the second catheter 116, or a combination of the these designs.
The impeller 118 can be configured to drive forward flow by creating openings in the motor 122 side of the impeller 118 and beveling the surfaces around the openings to form propeller-type geometries within the impeller 118. Thus, a single motor 122 and impeller 118 can perform all the fluid forcing required by the filter assembly 100. In another embodiment, a second motor and pump (not shown), or at least a second pump (not shown) operated by the same motor 122 causes fluid flow within the liquid return line 138. Flow rates within the liquid return line 138 can range between 0.5-cc per minute and 100-cc per minute. A separate liquid infusion port (not shown) can be operably connected to a hanging bag or source of non-cellular prime (not shown) such as saline, but this is not required for operation of the filter assembly 100 since all liquid can be drawn from the catheter or the initial filter assembly priming step.
In an embodiment, the impeller 118 can be housed within the chamber 104 without any impeller or motor shaft 148 passing through the wall of the chamber 104. This can be performed by embedding permanent magnets within the impeller 118 and having the motor 122 and shaft 148 turn complementary permanent magnets, which are affixed thereto. These permanent magnets can engage the impeller, by means of magnetic fields, through the walls of the chamber 104 and generate rotational motion of the impeller 118. The magnetic field interacts with the magnets within the impeller 118 and causes the impeller 118 to rotate at the same rate as that of the motor 122. The magnetic driver (not shown) is preferably a bar magnet that spins about its central region with north and south poles diametrically opposed and equidistant from the center of rotation. Typical permanent magnets are fabricated from materials such as, but not limited to, neodymium iron boron, iron, ceramics, samarium cobalt and the like. Materials that are magnetically attracted to a magnet include, but are not limited to, iron or metallic alloys of iron. The magnetic driver (not shown) is desirable because it allows for a sealed chamber 104.
All components of the blood air removal system 100 can be fabricated preferably from biocompatible materials, which are sterilizable using either ethylene oxide, gamma irradiation, electron beam irradiation, or the like. The blood air removal system 100 can be provided separately for attachment to a first catheter or sheath 140, it can be pre-attached thereto, or it can be provided in a kit, separately attached but provided therewith. The blood air removal filter system 100 is preferably provided sterile in an aseptic packaging system (not shown).
Optionally, the interior of the shell 102 of the blood filter 100 can be treated or coated with an anti-thrombogenic material such as heparin and a bonding agent. The impeller 118 can be made from materials that include polycarbonate, polypropylene, polyethylene, polystyrene, polyvinyl chloride, fluorinated ethylene polymer (FEP), polysulfone, polytetrafluoroethylene (PTFE), and the like.
The air vent port 228 is affixed to the shell 226 and is operably connected to the chamber 202 at or near the top of the chamber 202. The gas vent 224 is affixed to the top of the blood air separation chamber 204, which is affixed to the air vent port 228. The inlet side of the liquid return line 208 is affixed at or near to the bottom of the blood air separation chamber 204. The outlet side of the liquid return line 208 is affixed to the motor driven pump 206. The motor driven pump 206 is operably connected to the battery 218 by the electrical bus 220 and the on-off switch 222 is operably connected to the electrical bus 220 to provide a means for turning the motor driven pump 206 on and off. The outlet of the motor driven pump 206 is physically and operably connected to the inlet of the pump return line 210. The outlet of the pump return line 210 is physically affixed to the shell 226 and operably connected to the chamber 202.
The second catheter inlet port 230 is affixed to the shell 226 and comprises a central lumen, which is operably connected to the chamber 202 near the bottom of the chamber 202. The inlet valve 212 is affixed to the second catheter inlet port 230 and comprises a central lumen operably connected to the central lumen of the second catheter inlet port 230. The second catheter outlet port 236 is affixed to the shell and further comprises a lumen that is operably connected to the chamber 202 near the bottom. The second catheter outlet port 236 is affixed to the outlet valve 214 and to the first catheter connector 234. The first catheter connector 234 is affixed or reversibly coupled to the first catheter 232. The second catheter outlet port 236 can comprise a funnel-shaped or beveled entrance, or other type of guide structure 238, to coerce the second catheter shaft 140 to becoming coaxially aligned, should the second catheter shaft 140 become bent out of the axis slightly during insertion.
The shell 226 and other components of the blood air filter system 200 can be fabricated from the same materials as those used in the embodiment 100 shown in
The method of operation of the blood air filter system 200 is that it can be affixed to the proximal end of the first catheter 232. It can be primed and purged of air with saline through the gas vent 224. The motor driven pump 206 is turned on with the on-off switch 210. Flow is generated within the system to pull liquid out of the chamber 202 through the air vent port 228, and then pump liquid back into the chamber 202 through the pump return line 210, wherein air will separate in the air separation chamber 204 due to buoyant effects. Since the air vent port 228 is at the top of the chamber 202 any air in the chamber will preferentially collect near the air vent port 228 and be withdrawn from the chamber 202. Blood and other liquids, separated from the air in the air separation chamber 204 are returned to the chamber 202 by the motor driven pump 206.
The motor driven pump 206 can operate at voltages ranging between 1.5 and 24 volts DC and preferably between 1.5 and 6 volts DC. The battery 218 can match the voltage needs of the motor driven pump 206 and can operate for periods of up to 12 hours, preferably at least up to 6 hours once switched on. The system 200 is preferably disposable and is provided sterile in aseptic packaging similar to that described for the filter system 100 of
The ultrasound transducers 342 and 344 can be affixed to the second catheter outlet port 308 and the second catheter inlet port 310, respectively and can detect the presence of air or gas in the system, which is normally supposed to be filled only with liquid (blood, saline, etc.). Ultrasound signals can pass easily through liquids but they do not travel through gas well, so discrimination of the two phases is easily accomplished with ultrasound transducers. The ultrasound transducers 342 and 344 are wired to the ultrasound control unit 346 by an electrical bus (not shown). Power can be derived from the battery 324 or from another battery (not shown). The ultrasound control unit can display the presence of air by illuminating the warning light 348, sounding the audible signal 352, or both. Each transducer 342 and 344 can, in another embodiment, have a separate warning light, audible warning frequency, or both. Another ultrasound transducer (not shown) can be used to detect significant buildup of gas in the gas reservoir 336 such that the gas can be removed through the purge port 350.
Fluid being pumped back into the chamber 404 through the return inlet line 416 forms a fluid jet which, directed tangentially along the wall of the chamber 404, generates a circular flow pattern or vortex within the chamber 404. This circular flow pattern entrains air and bubbles toward the center due to the effects of air buoyancy acting in a centrifugal flow field. Thus air is moved away from the second catheter inlet port 410 and the second catheter outlet port 408, both of which are affixed to the shell 402 near the bottom and near the periphery of the chamber 402. Air can be entrained into the chamber 404 by insertion of the second catheter shaft 140 through the inlet valve 412, which is a hemostasis type valve as described in the embodiment shown in
The motor driven pump 406 can, in certain embodiments, serve to withdraw liquid from the distal end of the first catheter or sheath 114 all the way back to the gas collection chamber 422 where it can be removed from the system through the gas bleed 424. The power source 418 can be affixed directly to the shell 402 to minimize bulk. The on-off switch 512 for the motor driven pump 406 can be a separate on-off or on switch that runs until the battery power source 418 is depleted of energy. The on-off switch 512 can further be embedded within the second catheter inlet port 410, the second catheter outlet port 408. The on-off switch 512 can further be a light activated, ultrasonically activated by ultrasound transducers 342, 344, such as those described in
The gas purge port 424 can be monitored by an ultrasonic transducer to detect the presence of gas in the collection chamber 422 and audibly or visually signal the need to remove the gas. The gas purge port 424 can be terminated by a stopcock or other valve, such that application of a syringe or hypodermic needle can permit the removal of collected gas or air. The gas purge port 424 can further be interconnected to a pump system that automatically, or manually, actuates removes collected gas.
The filter 600 can be releasably affixed to the hub 602 of the cannula or first catheter 144 by means of a Luer lock 604, bayonet mount, threaded fitting, or the like. The Luer lock 604 is affixed to the distal end of the outlet port 606. The inlet port 608 is affixed to the hemostasis valve 312, which can comprise a duckbill valve, a Tuohy-Borst valve, a pinhole valve, a slit valve, a combination thereof, or similar. The motor drive 622, the shell 618, the impeller 610, and other components of the system can be fabricated from materials similar to those used for the filter embodiments illustrated in
Other aspects of the inventions include methods of use. In an exemplary embodiment, a sheath, such as a Mullins sheath is used to access the left atrium of the heart by way of femoral venous access via the Seldinger technique or similar. The Mullins-type sheath is advanced through the inferior vena cava into the superior vena cava. A transseptal needle, such as a Brockenbrough needle, is inserted through the Mullins-type sheath or catheter and aligned medially. The transseptal needle and sheath combination is withdrawn from the superior vena cava into the right atrium where the catheter, protecting the tip of the needle engages the fossa Ovalis. The needle is advanced out through the distal end of the Mullins-type sheath and through the fossa Ovalis. The Mullins sheath is advanced over the transseptal needle into the left atrium. The transseptal needle is removed and therapeutic or diagnostic catheters are inserted through the Mullins-type sheath into the left atrium. Procedures such as electrophysiology mapping, electrophysiology ablation of the heart, atrial appendage procedures including plugs, filters, and closure devices, mitral valve procedures., and the like can be performed through such an access procedure. The application of the air filter, described herein, to the proximal end of the Mullins-type sheath would significantly reduce the risk of air embolism in these procedures. The left atrium can expose the distal end of the catheter to low enough pressures to draw air into the left atrium through an inserted catheter, thus the need for such a prevention device. Other procedures where such an air embolism protection device would be beneficial includes central venous access catheters, cardiac access catheters and catheters used for cerebrovascular access.
The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is therefore indicated by the appended claims rather than the foregoing description. All changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope.
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